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Poriferous, LLC

FDA Regulatory Profile

Poriferous, LLC appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 20, 2016.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K152463SU-POR Patient-Specific Cranial Implant, SU-POR Patient-Specific Facial ImplantJanuary 20, 2016
K140437SU-POR SURGICAL IMPLANTJune 13, 2014

FDA data resources